The Efficacy of Using Patient-Derived Organoids to Predict Treatment Response in Colorectal Cancer

Author:

Su Chang12,Olsen Kelly A.1ORCID,Bond Catherine E.1,Whitehall Vicki L. J.123

Affiliation:

1. Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute, Herston 4006, Australia

2. Faculty of Medicine, The University of Queensland, Herston 4006, Australia

3. Conjoint Internal Medicine Laboratory, Pathology Queensland, Herston 4006, Australia

Abstract

Colorectal cancer is an important cause of morbidity and mortality worldwide. The current treatment landscape includes chemotherapy, targeted therapy, immunotherapy, radiotherapy, and surgery. A key challenge to improving patient outcomes is the significant inter-patient heterogeneity in treatment response. Tumour organoids derived from the patients’ tumours via surgically resected or endoscopically biopsied tissue, have emerged as promising models for personalised medicine. This review synthesises the findings, to date, of studies which have explored the efficacy of ex vivo organoid sensitivity testing for predicting treatment response. Most studies have focused on predicting the response to standard-of-care radiotherapy and chemotherapy options. There is strong evidence to support organoid sensitivity testing of ionising radiation, 5-fluorouracil, and irinotecan, and to a lesser extent, oxaliplatin and TAS-102. Fewer studies have used organoids to identify patients who are likely to benefit from novel treatment options that otherwise remain in clinical trials. This review also summarises recent advancements in organoid culture to include non-epithelial components of the tumour microenvironment, to allow testing of immunotherapy and certain targeted therapy options. Overall, further prospective trials will support the implementation of organoid-based personalised medicine for colorectal cancer patients in the future.

Funder

Medical Research Future Fund Rapid Applied Research Translation Program

Garry Whyte Sea Angel PAF

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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